NDC 76144-913 Paulas Choice Calm Redness Relief Spf 30 Mineral Moisturizer (normal To Dry)
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 76144-913?
What are the uses for Paulas Choice Calm Redness Relief Spf 30 Mineral Moisturizer (normal To Dry)?
Which are Paulas Choice Calm Redness Relief Spf 30 Mineral Moisturizer (normal To Dry) UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Paulas Choice Calm Redness Relief Spf 30 Mineral Moisturizer (normal To Dry) Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- SOY STEROL (UNII: PL360EPO9J)
- OAT (UNII: Z6J799EAJK)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- UBIDECARENONE (UNII: EJ27X76M46)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EICOSYL POVIDONE (UNII: XQQ9MKE2BJ)
- SUPEROXIDE DISMUTASE (SACCHAROMYCES CEREVISIAE) (UNII: W2T4YRA9AD)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ALLANTOIN (UNII: 344S277G0Z)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- WATER (UNII: 059QF0KO0R)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- APRICOT KERNEL OIL (UNII: 54JB35T06A)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".